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Methanone, [4-(methylthio)phenyl]-2-pyridinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95898-77-4

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95898-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95898-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,9 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95898-77:
(7*9)+(6*5)+(5*8)+(4*9)+(3*8)+(2*7)+(1*7)=214
214 % 10 = 4
So 95898-77-4 is a valid CAS Registry Number.

95898-77-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylsulfanylphenyl)-pyridin-2-ylmethanone

1.2 Other means of identification

Product number -
Other names Methanone,[4-(methylthio)phenyl]-2-pyridinyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95898-77-4 SDS

95898-77-4Relevant academic research and scientific papers

Efficient Selenium-Catalyzed Selective C(sp3)?H Oxidation of Benzylpyridines with Molecular Oxygen

Jin, Weiwei,Zheng, Poonnapa,Wong, Wing-Tak,Law, Ga-Lai

supporting information, p. 1588 - 1593 (2017/05/05)

An efficient selenium-catalyzed direct oxidation of benzylpyridines in aqueous DMSO has been successfully developed by using molecular oxygen as the oxidant. A variety of benzoylpyridines with broad functional group tolerance were obtained in modest to excellent yields and with exclusive chemoselectivity. (Figure presented.).

Synergistic H4NI-AcOH Catalyzed Oxidation of the Csp3-H Bonds of Benzylpyridines with Molecular Oxygen

Ren, Lanhui,Wang, Lianyue,Lv, Ying,Li, Guosong,Gao, Shuang

supporting information, p. 2078 - 2081 (2015/05/13)

The oxidation of benzylpyridines forming benzoylpyridines was achieved based on a synergistic H4NI-AcOH catalyst and molecular oxygen in high yield under solvent-free conditions. This is the first nonmetallic catalytic system for this oxidation transformation using molecular oxygen as the oxidant. The catalytic system has a wide scope of substrates and excellent chemoselectivity, and this procedure can also be scaled up. The study of a preliminary reaction mechanism demonstrated that the oxidation of the Csp3-H bonds of benzylpyridines was promoted by the pyridinium salts formed by AcOH and benzylpyridines. The synergistic effect of H4NI-AcOH was also demonstrated by control experiments. (Figure Presented).

Synthesis of aryl(di)azinyl ketones through copper- and iron-catalyzed oxidation of the methylene group of aryl(di)azinylmethanes

De Houwer, Johan,Abbaspour Tehrani, Kourosch,Maes, Bert U. W.

supporting information; experimental part, p. 2745 - 2748 (2012/04/10)

Sustainable Oxidations: An oxidation method to transform aryl(di)azinylmethanes into aryl(di)azinyl ketones is described. Base metals (copper and iron) as catalysts in combination with O2 as the oxidant are used, which makes this method sustainable. The utility of this method is illustrated by the synthesis of 6-(4-methylbenzoyl)pyridine-2-carbaldehyde, which is an intermediate in the preparation of the drug Acrivastine. Copyright

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